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GD-Anidulafungin: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx) Current status: Cancelled Pre Market
Strength:
100 mg
Active ingredient:

Patient Medication Information: uses, side effects, how to take - GD-Anidulafungin

ABOUT THIS MEDICATION

What the medication is used for:

GD-Anidulafungin belongs to a group of medicines called echinocandins. These medicines are used to treat serious fungal infections.

GD-Anidulafungin is prescribed to treat a type of fungal infection called invasive candidiasis (including candidemia). The infection is caused by fungal cells (yeasts) called Candida.

What it does:

Fungal cells exposed to GD-Anidulafungin have incomplete or defective cell walls making them fragile or unable to grow, thereby killing the cells and reducing the infection.

When it should not be used:

If you are allergic (hypersensitive) to anidulafungin, other echinocandins, or any of the other ingredients of GD-Anidulafungin (Fructose, Mannitol, Polysorbate 80, Tartaric acid, Sodium hydroxide or Hydrochloric acid).

What the medicinal ingredient is:

The active ingredient is anidulafungin.

What the important non-medicinal ingredients are:

Fructose, Mannitol, Polysorbate 80, Tartaric acid, Sodium hydroxide (for pH-adjustment), Hydrochloric acid (for pH-adjustment)

What dosage form it comes in:

GD-Anidulafungin is marketed as a carton containing 1 vial of 100 mg powder for solution for infusion.

WARNINGS AND PRECAUTIONS

BEFORE you use GD-Anidulafungin talk to your doctor or pharmacist:

  • If you have been told by your doctor that you have an intolerance to some sugars. Patients with rare hereditary problems of fructose intolerance should not take this medicine. This medicinal product contains fructose.
  • If you become pregnant while taking GD-Anidulafungin:

    GD-Anidulafungin should not be taken during pregnancy, unless indicated by your doctor. Effective contraception should be used in women of childbearing potential.

  • If you are breast-feeding or planning to breast feed . You and you doctor will decide whether you should take this medication or not while breastfeeding or whether you should discontinue breastfeeding.
  • If you have any allergies to this drug or its ingredients or components of the container.
  • If you have liver problems.

INTERACTIONS WITH THIS MEDICATION

Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.

It is not expected that GD-Anidulafungin will interact with other medications or that any adjustments will be necessary to other medicines you may be taking. However, do not start or stop any other medications without your doctor or pharmacist’s approval.

PROPER USE OF THIS MEDICATION

GD-Anidulafungin will always be prepared and given to you by a doctor or a healthcare professional.

Usual adult dose:

GD-Anidulafungin should be administered once a day, by slow infusion into your vein over approximately 1.5 to 3 hours. The treatment starts with a loading dose of 200 mg on the first day, then with subsequent daily maintenance dose of 100 mg. GD-Anidulafungin should not be given to patients under 18 years of age.

Your doctor will determine the duration of your treatment and how much anidulafungin you will receive each day, and will monitor your response and condition.

Overdose:

Your doctor will monitor your response and condition to determine what GD-Anidulafungin treatment is needed. However, if you are concerned that you may have been given too much GD-IMPORTANT: PLEASE READ

GD-Anidulafungin (anidulafungin) - Product Monograph Page 28 of 28 Anidulafungin, tell your doctor or another healthcare professional immediately.

Missed Dose:

As you will be given this medicine under close medical supervision, it is unlikely that a dose would be missed. However tell your doctor or pharmacist if you think that a dose has been forgotten.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

Like all medicines, GD-Anidulafungin can cause side effects, although not everybody gets them.

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM
Symptom / effect

Talk with your

doctor or pharmacist

Stop taking drug and call your doctor or pharmacist
Only if severeIn all cases
Common

-Hypokalemia (low potassium levels) and

symptoms such as muscle

weakness, and cramping,

irregular heart beat, frequent urination

√
Uncommon
  • High blood pressure

-Liver problems (hepatitis) with symptoms such as persistent abdominal pain, nausea,

Vomiting

  • Anaphylactic (allergic)

reactions with symptoms such as rash, hives, low blood

pressure,

fainting,

swelling of

mouth, throat and extremities, weakness,

difficulty in breathing

√

√

√

√
  • A common effect is diarrhea.
  • Uncommon side effects include headache, rash, itching, flushing, eye pain, infusion site reaction

If these reactions become troublesome, contact your doctor

This is not a complete list of side effects. For any unexpected effects while taking GD-Anidulafungin, contact your doctor or pharmacist.

HOW TO STORE IT

Unreconstituted vials of GD-Anidulafungin are stored in a refrigerator (2-8°C). Do not freeze.

Keep out of the reach and sight of children.

Do not use GD-Anidulafungin after the expiry date which is stated on the label.

REPORTING SUSPECTED SIDE EFFECTS

You can report any suspected adverse reactions associated with the use of health products to the Canada Vigilance Program by one of the following 3 ways:

  • Report online at www.healthcanada.gc.ca/medeffect
  • Call toll-free to 1-866-234-2345
  • Complete a Canada Vigilance Reporting Form and:

    • Fax toll-free to 1-866-678-6789, or
    • Mail to: Canada Vigilance Program

      Health Canada

      Postal Locator 0701C

      Ottawa, ON K1A 0K9

Postage paid labels, Canada Vigilance Reporting Form and the adverse reaction reporting guidelines are available on the MedEffectTM Canada Web site at

www.healthcanada.gc.ca/medeffect.

NOTE: Should you require information related to the management of the side effect, please contact your health care provider before notifying Canada Vigilance. The Canada Vigilance Program does not provide medical advice.

MORE INFORMATION

This document plus the full product monograph, prepared for health professionals can be found at:

http://www.pfizer.ca or by contacting the sponsor, GenMed, a Division of Pfizer Canada Inc., at 1-800-463-6001 (Medical Information).

Last revised: May 26, 2015

* GD is a trademark of Pfizer Canada Inc.

GenMed, a division of Pfizer Canada Inc., Licensee © Pfizer Canada Inc., 2015

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02441683

Revision date stated in the text: May 26, 2015

Found a mistake? Write to us via the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for GD-Anidulafungin

Rx or OTC
Prescription (Rx)?
DIN 02441683
Schedule(s) PRESCRIPTION
Active ingredient(s) Anidulafungin 100 MG
Dosage form(s) Powder For Solution
Route(s) of administration Intravenous
Drug class (WHO ATC)
  1. J Antiinfectives for systemic use
    1. J02 Antimycotics for systemic use
      1. J02A Antimycotics for systemic use
        1. J02AX Other antimycotics for systemic use
          1. J02AX06 Anidulafungin
Company GENMED A DIVISION OF PFIZER CANADA ULC
Current status Cancelled Pre Market
Current status date January 15, 2021

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.